C7, complement C7, 730

N. diseases: 16; N. variants: 11
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation disease BEFREE DNA polymorphism of the human complement component C7 gene in familial deficiencies. 1973405 1990